Canonical Allele Identifier: PA2827007063
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405944

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser477Asn
CA031083
NM_001318829.2:c.1430G>A